碘化丙啶
体内
人类白细胞抗原-DR
细胞培养
医学
单克隆抗体
抗体
人类白细胞抗原
体外
免疫学
细胞凋亡
抗原
癌症研究
程序性细胞死亡
分子生物学
生物
生物化学
遗传学
生物技术
作者
Carmelo Carlo‐Stella,Anna Guidetti,Massimo Di Nicola,Cristiana Lavazza,Loredana Cleris,Daniela Sia,Paolo Longoni,Marco Milanesi,Michele Magni,Zoltan A. Nagy,Paolo Corradini,Antonino Carbone,Franca Formelli,Alessandro M. Gianni
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2007-04-01
卷期号:67 (7): 3269-3275
被引量:18
标识
DOI:10.1158/0008-5472.can-06-3744
摘要
To investigate the therapeutic activity of the fully human anti-HLA-DR antibody 1D09C3 in multiple myeloma (MM), we reevaluated HLA-DR expression on CD138(+) cells, analyzed the capacity of IFN-gamma to up-regulate HLA-DR expression on MM cell lines, and tested the in vitro and in vivo activity of 1D09C3 alone or in combination with IFN-gamma. CD138(+)HLA-DR(+) cells were detected in 31 of 60 patients, with 15 of 60 patients having >/=20% CD138(+)HLA-DR(+) cells (median, 50%; range, 23-100). Because primary plasma cells cannot be efficiently cultured in vitro, we used a panel of MM cell lines with a dim/negative to bright HLA-DR expression to evaluate 1D09C3-induced cell death. Annexin V/propidium iodide (PI) staining showed that 1D09C3-induced cell death correlated with constitutive HLA-DR expression. Induction of HLA-DR by IFN-gamma restored the sensitivity of HLA-DR dim cell lines to 1D09C3. In vivo, the combined IFN-gamma/1D09C3 treatment significantly increased the median survival of nonobese diabetic/severe combined immunodeficient mice xenografted with KMS-11 cell line, compared with controls (147 versus 48 days, P = 0.0001) or mice receiving 1D09C3 alone (147 versus 92 days, P = 0.03). The better therapeutic activity of IFN-gamma/1D09C3 treatment over 1D09C3 alone was further shown by a 2-fold increase of mice being disease-free at 150 days after xenograft (47% versus 25%). No mice experienced any apparent treatment-related toxicity. Our data show that (a) one fourth of MM patients express HLA-DR on CD138(+) cells and (b) IFN-gamma-induced up-regulation of HLA-DR results in a potent enhancement of the in vivo antimyeloma activity of 1D09C3.
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